New Zealand Medical Device Reporting

At Manningham Medical Centre, you can find all the data about New Zealand Medical Device Reporting. We have collected data about general practitioners, medical and surgical specialists, dental, pharmacy and more. Please see the links below for the information you need.

Adverse Event Reporting - Medsafe

https://www.medsafe.govt.nz/regulatory/DevicesNew/9AdverseEvent.asp

Medical Devices Home Page - Medsafe

https://medsafe.govt.nz/devices/devices-landing.asp

Information for Medical Device Suppliers. Medicines and Medical Devices Recall Code. Device Information. New Zealand Definitions. Medical Device Legislation. Overseas …

Regulatory Guidance for Medical Devices - Medsafe

https://www.medsafe.govt.nz/regulatory/devicesnew/industry.asp

Advertising of Medical Devices; Conducting Clinical Trials in New Zealand; Surgical Mesh. Adverse Event Reporting; Medsafe Actions; Information for Healthcare …

Medsafe Home Page

https://medsafe.govt.nz/index.asp

What's New Act on side effects to medicines Taking a medicine? Tell you doctor if you experience any side effects. You can also report side effects to medicines Consumers …

Regulatory Requirements for Sponsors - Medsafe

https://www.medsafe.govt.nz/regulatory/devicesnew/3-6RegulatoryRequirements.asp

This Regulation requires a sponsor to notify a medical device to the database within 30 working days of becoming the sponsor. The interpretation of the 30 working day …

Therapeutic products regulatory regime | Ministry of …

https://www.health.govt.nz/our-work/regulation-health-and-disability-system/therapeutic-products-regulatory-regime

This will include: regulating medicines from general sale products like paracetamol to gene, cell and tissue therapies, and medical devices that range from …

Medical device registration and approval in New Zealand - Emergo

https://www.emergobyul.com/services/medsafe-medical-device-registration-new-zealand

New Zealand market notification process for medical devices Although pre-market approval of medical devices is not necessary in New Zealand, market entry does require listing …

Adverse Reaction Reporting - Medsafe

https://www.medsafe.govt.nz/safety/ADR-reporting.asp

Medical Device Adverse Event Reporting Information on reporting an adverse event or a quality issue associated with a medical device. More... How to Report a Problem How to …

Recalls and Corrective Actions - Medsafe

https://www.medsafe.govt.nz/regulatory/devicesnew/8Recalls.asp

Medsafe should be informed as soon as possible and advised of the proposed actions for New Zealand. Drafting a recall action notice As the legal representative of the …

Report a Problem - Medsafe

https://www.medsafe.govt.nz/safety/report-a-problem.asp

Download a healthcare professional reporting form and submit to CARM via email, fax or mail (NZPhvC, University of Otago Medical School, PO Box 913, Dunedin 9054). Email: …

Need more information about New Zealand Medical Device Reporting?

At Manningham Medical Centre, we collected data on more than just New Zealand Medical Device Reporting. There is a lot of other useful information. Visit the related pages or our most popular pages. Also check out our Doctors page.